Abstract
Sotos syndrome is a rare genetic disorder presenting with craniofacial abnormalities, profound hypotonia, and cardiac abnormalities, giving rise to several potential challenges and concerns for an anesthesiologist. When preparing for a Sotos syndrome patient’s case, we consulted the literature for precedents on how to plan the anesthetic, to which we were only able to find a few reports and nothing in the age group our patient fell within. We present our case of an adult in addition to examining the previous cases so as to document a precedent when encountering patients with this syndrome in the operating room. We describe a unique case of a nonverbal adult with hypotonia and severe craniofacial abnormalities who successfully underwent multiple dental extractions under general anesthesia, with no complications other than a delay of emergence attenuated by naloxone. Our case and the seven previous documented cases over the past several decades demonstrate anesthesia, including paralytics and intubation itself safe despite obvious concerns given the common features of the syndrome for both pediatric patients and the one adult we described in this report.
1. Introduction
Sotos syndrome, also known as cerebral gigantism, is a rare genetic disorder with an estimated prevalence at birth of 1 in 14,000 [1]. An overwhelming majority of cases are linked to mutations in the NSD1 gene located on chromosome 5 [2]. Children with this syndrome typically have distinctive facial features, macrocephaly, learning disabilities, and advanced bone age. Characteristic facial features include frontal bossing, prominently long narrow chin, and downslanting palpebral fissures [3]. Patients also present with hypotonia, cardiac abnormalities, scoliosis, renal anomalies, and behavioral problems compounding the learning difficulties. As children with Sotos syndrome age, their physical abnormalities can become more subtle. Adults with Sotos syndrome can manifest a wide spectrum of disease where some are completely dependent on care givers while others are able to live independently [3].
We present a case of an 18-year-old male with Sotos syndrome who had multiple dental extractions under general anesthesia and summarize previously published cases of Sotos syndrome anesthetics. In searching the literature, we found seven case reports describing anesthesia in children with Sotos syndrome [4–10]. However, we were not able to find any reports on the anesthetic management of adults with Sotos syndrome. As Sotos syndrome patients age, it is worth revisiting their anesthetic management and documenting any precedents available. Authors obtained permission and written informed consent from the patient’s mother presented in this case report.
2. Case Presentation
An 18-year-old male presented for dental restorations and extractions. His medical history included Soto syndrome, Guillain–Barre syndrome, epilepsy, scoliosis, stage III chronic kidney disease (associated with a solitary dysplastic kidney), and autism spectrum disorder. Home medications included sertraline, risperidone, gabapentin, divalproex, diazepam, benztropine, fluticasone, and an albuterol inhaler, and no history of any surgical procedures. A 2-year-old transthoracic echocardiogram was unremarkable. Physical exam revealed an elongated mandible, frontal bossing, significant hypotonia and kyphosis. He was nonverbal, agitated, and uncooperative, attempting to hit preoperative nurses. Due to COVID-19, his mother was unable to accompany and console him en route to the operating room. Because the patient was nonverbal, the mother signed consent on the patient’s behalf for publication of the case.
He was premedicated with 15 mg of midazolam via a gastric tube prior to transport to the operating room, which sufficiently placated the agitation. In the operation room, standard monitors were placed and anesthesia induced using nitrous oxide and sevoflurane via the mask without difficulty. Following induction, peripheral intravenous access was established, and propofol 50 mg and rocuronium 30 mg were administered in preparation for intubation. Direct laryngoscopy was performed using a Miller 2 blade. A Cormack-Lehane grade 1 view was obtained on the first attempt, and a 6.0 endotracheal tube was placed without difficulty. Anesthesia was maintained with an oxygen/air mixture and sevoflurane, and a single dose hydromorphone 0.5 mg was administered intravenously at procedure start.
The patient’s intraoperative course was unremarkable. No additional neuromuscular blocking agent or narcotic was administered. At the procedure end, sugammadex 200 mg IV was administered after a train-of-four assessment demonstrated 1/4 twitches with significant fade. Despite full reversal of neuromuscular blockade (4/4 twitches without fade) and an end-tidal sevoflurane concentration of 0.3%, the patient remained unresponsive and without spontaneous respiratory effort. Following three doses of Narcan 0.4 mg intravenously, the patient had return of spontaneous respirations with good tidal volumes and rate. Patient was extubated without incident and transported to the postanesthesia care unit on a non-rebreather mask. The patient had an unremarkable postoperative course and was discharged to home 60 minutes later.
3. Discussion
Sotos syndrome has a number of phenotypes that could be of concern to an anesthesiologist. These include craniofacial abnormalities, muscular hypotonia, behavioral disorders, and potential cardiac and renal abnormalities. Before discussing an anesthetic plan, a literature review was done to look for precedents given the concerning features of Sotos syndrome, as the syndrome was unknown to us before taking care of this patient. Our patient manifested more severe diseases with significant scoliosis, hypotonia, kyphosis, and a single dysplastic kidney. He was also nonverbal and had a history of aggressive behavior. An airway exam was not possible due to agitation, so adjuncts to manage a difficult airway were readily available such as supraglottic airways, video-laryngoscopy, fiberoptic bronchoscope, and bougies in the event that the craniofacial abnormalities provided a difficult airway. However, the patient had an easy mask airway and easy intubation with direct laryngoscopy. This is consistent with the experience of other authors in the management of airways in children with Sotos syndrome [4–10], wherein there was no difficulty with intubation. Despite preexisting hypotonia, we also did not observe any excessive sensitivity to nondepolarizing neuromuscular blockade or delay in return of neuromuscular function following administration of sugammadex. This is also consistent with published reports in the pediatric population [4, 7, 8], wherein there were no issues with neuromuscular blockade despite pronounced hypotonia.
Our review of the literature revealed case reports describing anesthesia in children with Sotos syndrome [5–10], none of which had any anesthetic complications, all summarized in Table 1. This is being the 8th such report without any major incident with regard to hypotonia or airway. Regardless, we recommend close train-of-four monitoring and use of reversal agents as appropriate. We also recommend careful titration of opioids given the potential for sensitivity. Given the rarity of the syndrome, we hope this report will provide a precedent for the anesthetic management of an adult with Sotos syndrome and a means to quickly see previously documented anesthetic management.
Data Availability
The data used to support the findings of this case report are included within the article.
Conflicts of Interest
The authors declare that there are no conflicts of interest.